Canonical Allele Identifier: CA391298720
Gene: NIPA1 HGNC NCBI

Linked Data

gnomAD v4: 15-22786771-A-G
MyVariant Identifiers: chr15:g.23086297T>C (hg19) chr15:g.22786771A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786771A>G , CM000677.2:g.22786771A>G GRCh38
NC_000015.9:g.23086297T>C , CM000677.1:g.23086297T>C GRCh37
NC_000015.8:g.20637738T>C NCBI36
NG_009056.1:g.5547A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.9:c.115A>G MANE Select ENSP00000337452.4:p.Ser39Gly
ENST00000337435.8:c.115A>G ENSP00000337452.4:p.Ser39Gly
ENST00000437912.6:c.-48+12458A>G ENSP00000393962.2:n.-48+12458A>G
ENST00000559448.5:c.5A>G
ENST00000560069.5:n.31+523A>G
ENST00000560105.1:n.14A>G
ENST00000561183.5:c.-48+523A>G ENSP00000453722.1:n.-48+523A>G
NM_001142275.1:c.-48+523A>G NP_001135747.1:n.-48+523A>G
NM_144599.4:c.115A>G NP_653200.2:p.Ser39Gly
NM_144599.5:c.115A>G MANE Select NP_653200.2:p.Ser39Gly
Search 100 bp 5'
Search 100 bp 3'